FDA Adverse Event Injury Summary report: N

QUALA

MDR report key: 211817 · Received February 26, 1999

Report

Report Number
1412902-1999-00002
Event Type
Injury
Date Received
February 26, 1999
Date of Event
October 28, 1998
Report Date
January 22, 1999
Manufacturer
MPL TECHNOLOGIES
Product Code
DZM
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
KY, US
Reporter Occupation
DENTIST

Narratives

Description of Event or Problem · 1

ORAL SURGERY WAS NEEDED TO REMOVE A BROKEN NEEDLE FROM A PT'S GUM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 QUALA DENTAL NEEDLE DZM MPL TECHNOLOGIES UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Required Intervention